Structural studies of an engineered zinc biosensor reveal an unanticipated mode of zinc binding

Protein engineering was used previously to convert maltose-binding protein (MBP) into a zinc biosensor. Zn2+ binding by the engineered MBP was thought to require a large conformational change from open to closed, similar to that observed when maltose is bound by the wild-type protein. We show that although this re-designed MBP molecule binds Zn2+ with high affinity as previously reported, it does not adopt a closed conformation in solution as assessed by small-angle X-ray scattering. High-resolution crystallographic studies of the engineered Zn2+-binding MBP molecule demonstrate that Zn2+ is coordinated by residues on the N-terminal lobe only, and therefore Zn2+ binding does not require the protein to adopt a fully closed conformation. Additional crystallographic studies indicate that this unexpected Zn2+ binding site can also coordinate Cu2+ and Ni2+ with only subtle changes in the overall conformation of the protein. This work illustrates that the energetic barrier to domain closure, which normally functions to maintain MBP in an open concentration in the absence of ligand, is not easily overcome by protein design. A comparison to the mechanism of maltose-induced domain rearrangement is discussed. (c) 2005 Elsevier Ltd. All rights reserved.